null

SMILES CN(C)C[C@H]1CC2[C@H](O1)c1cc(F)ccc1Oc1ccccc21

InChI Key InChIKey=LGHLMADLDHUIJY-MQSINFNDSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 9 hits for monomerid = 50162960   

TargetTransporter(Rattus norvegicus)
Johnson & Johnson Pharmaceutical Research & Development

Curated by ChEMBL
LigandPNGBDBM50162960((11-Fluoro-2,3,3a,12b-tetrahydro-1,8-dioxa-dibenzo...)copy SMILEScopy InChI
Affinity DataKi:  3.60nMAssay Description:Inhibition of [3H]-nisoxetine binding to rat Norepinephrine transpoterMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MC8ZHBPubMed
Target5-hydroxytryptamine receptor 2C(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research & Development

Curated by ChEMBL
LigandPNGBDBM50162960((11-Fluoro-2,3,3a,12b-tetrahydro-1,8-dioxa-dibenzo...)copy SMILEScopy InChI
Affinity DataKi:  4.30nMAssay Description:Inhibition of [3H]-mesulergine binding to human 5-hydroxytryptamine 2C receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MC8ZHBPubMed
TargetHistamine H1 receptor(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research & Development

Curated by ChEMBL
LigandPNGBDBM50162960((11-Fluoro-2,3,3a,12b-tetrahydro-1,8-dioxa-dibenzo...)copy SMILEScopy InChI
Affinity DataKi:  7.5nMAssay Description:Inhibition of [3H]-pyrilamine binding to human Histamine H1 receptor More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MC8ZHBPubMed
TargetD(3) dopamine receptor(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research & Development

Curated by ChEMBL
LigandPNGBDBM50162960((11-Fluoro-2,3,3a,12b-tetrahydro-1,8-dioxa-dibenzo...)copy SMILEScopy InChI
Affinity DataKi:  31nMAssay Description:Inhibition of [125I]-iodosulpride binding to human Dopamine receptor D3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MC8ZHBPubMed
TargetD(2) dopamine receptor(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research & Development

Curated by ChEMBL
LigandPNGBDBM50162960((11-Fluoro-2,3,3a,12b-tetrahydro-1,8-dioxa-dibenzo...)copy SMILEScopy InChI
Affinity DataKi:  32nMAssay Description:Inhibition of [3H]-spiperone binding to human Dopamine receptor D2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MC8ZHBPubMed
Target5-hydroxytryptamine receptor 7(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research & Development

Curated by ChEMBL
LigandPNGBDBM50162960((11-Fluoro-2,3,3a,12b-tetrahydro-1,8-dioxa-dibenzo...)copy SMILEScopy InChI
Affinity DataKi:  80nMAssay Description:Inhibition of [3H]-5-HT binding to human 5-hydroxytryptamine 7 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MC8ZHBPubMed
TargetAlpha-2C adrenergic receptor(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research & Development

Curated by ChEMBL
LigandPNGBDBM50162960((11-Fluoro-2,3,3a,12b-tetrahydro-1,8-dioxa-dibenzo...)copy SMILEScopy InChI
Affinity DataKi:  200nMAssay Description:Inhibition of [3H]-rauwolscine binding to Alpha-2C adrenergic receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MC8ZHBPubMed
TargetAlpha-2A adrenergic receptor(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research & Development

Curated by ChEMBL
LigandPNGBDBM50162960((11-Fluoro-2,3,3a,12b-tetrahydro-1,8-dioxa-dibenzo...)copy SMILEScopy InChI
Affinity DataKi:  269nMAssay Description:Inhibition of [3H]-rauwolscine binding to Alpha-2A adrenergic receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MC8ZHBPubMed
Target5-hydroxytryptamine receptor 2A(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research & Development

Curated by ChEMBL
LigandPNGBDBM50162960((11-Fluoro-2,3,3a,12b-tetrahydro-1,8-dioxa-dibenzo...)copy SMILEScopy InChI
Affinity DataKi: >5.45E+3nMAssay Description:Inhibition of [125I]-R91150 binding to human 5-hydroxytryptamine 2A receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MC8ZHBPubMed